Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: EQH FDA class 1

Source, Carrier, Fiberoptic Light

Ear, Nose, Throat

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The fiberoptic light source and carrier is a device that generates and transmits light via fiber optic cables to illuminate body cavities during ENT surgical or diagnostic procedures. It is classified as FDA Class 1, indicating low risk and requiring only general controls without a premarket notification. The product code is EQH, regulated under 21 CFR 874.4350 in the Ear, Nose, Throat specialty. No special regulatory flags apply.

510(k) Clearances

49 matches
K Number
Device Name
WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT
JED-LIGHT FIBEROPTIC LIGHT SOURCE
COLD LIGHT SOURCE LOS 150
BATTERY POWERED, DISPOSABLE ENDOSCOPE LIGHT SOURCE
GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHT
GM OPTI*CAM CAMERA WITH ENT FIBER OPTIC LIGHT
SAPHIRE PLUS SURGICAL MIRROR
MID LABS TWIN ILLUMINATOR
ASPIRATING ENDO OCULAR PROBE
FIBEROPTIC LIGHTSOURCES AND CARRIERS
THROAT-A-SCOPE
DISPOSABLE ENDOILLUMINATOR
LX 150 LIGHT SOURCE
GRIESHABER THREE FUNCTION MANIPULATOR
GRIESHABER TWO FUNCTION MANIPULATOR
ASPIRATING ENDO OCULAR PROBE
KAPS 90 DEGREE FIBEROPTIC ADAPTOR
FIBER OPTIC UNIVERAL CABLES, SCOPE ADAP., LT.SOURC
OMNIVIEW(TM) OPHTHALMIC FIBERENDO W/NEEDLEHOLDER
RIVER MEDICAL MICRODRILL SYSTEM
F.T.I. MEDICAL LIGHT GUIDE
SUMMIT TECH 19/20 GAUGE OPHTHALMIC FIBERENDOSCOPE
FIBER OPTIC LIGHT SOURCE
FIBEROPTIC LIGHT SOURCE, FOI-1A
LUXTEC FIBEROPTIC CABLES
LUXTEC, KILLIAN AND VIENNA NASAL SPECULUMS
FRAZIER SUCTION TUBE
ZIMMER VIDEO PRODUCTS AUTOMATIC LIGHT SOURCE
BRIMFIELD FIBEROPTIC LIGHT SCOURCE
VENT TUBE FORCEPS
T-TUBE INSERTER
MICROSURGICAL GAUGE
MCGEE 26GA. SUCTION TUBE
LARYNGEAL SPATULAS
FIBEROPTIC LIGHT CARRIERS
ADAPTOR FOR FIBEROPTIC LIGHT SOURCE
FIBEROPTIC LIGHT CARRIERS
NASAL INSTRUMENTS
DALE COMBO TRACHEOSTOMY TUBE HOLDER
FIBER OPTIC ADAPTER #60-0896
FIBER OPTIC LIGHT GUIDE #60-0767
FIBER OPTIC ADAPTER CAT#60-0898
FIBER OPTIC LIGHT GUIDE CAT#60-0768
FIBER OPTIC ADAPTER #60-0894
FIBER OPTIC ADAPTER #60-0897
FIBER OPTIC ADAPTER #60-0892
FIBER OPTIC ADAPTER #60-895
FIBER OPTIC LIGHT SOURCE
ADAPTER/STANDARD FIBER OPTICS LIGHT

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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